Gene table: search width pubmed_id = 23455423


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2 - (AD)
5.38
23455423
HNRNPA2B1 (7q15.2)
Hetergeneous nuclear ribonucleoprotein A2/B1
* Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia - IBMPFD2
* Oculopharyngeal muscular dystrophy related to HNRNPA2B1